Canonical Allele Identifier: PA2828893889
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 181543

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369323.1:p.Ser1103Trp
CA297231
NM_001382394.1:c.3308C>G